Human chromosome 17 in essential hypertension.

doi:10.1046/j.1469-1809.2003.t01-1-00002.x

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Article

Human chromosome 17 in essential hypertension.

Annals of human genetics - 1 Mar 2003

Knight J, Munroe P B, Pembroke J C, Caulfield M J

Abstract excerpt

Hypertension affects up to 30% of the adult population in Western societies and is a major risk factor for kidney disease, stroke and coronary heart disease. It is a complex trait thought to be influenced by a number of genes and environmental factors, although the precise aetiology remains unknown at this time. A number of methods have been successfully used to identify mutations that cause Mendelian traits and...

Topics

Animals
Blood Pressure
Chromosome Mapping
Chromosomes, Human, Pair 17
Disease Models, Animal
Genetic Linkage
Genetic Markers
Humans
Hypertension
Mice
Peptidyl-Dipeptidase A
Phenotype
Pseudohypoaldosteronism
Quantitative Trait Loci
Rats
Rats, Inbred SHR

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Open in PubMed

Identifiers

PMID: 12675695
DOI: 10.1046/j.1469-1809.2003.t01-1-00002.x

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